Goichiro Tamura, Dawne Olson, Joel Miron, Timothy G. Clark
{"title":"Tolloid-like 1 is negatively regulated by stress and glucocorticoids","authors":"Goichiro Tamura, Dawne Olson, Joel Miron, Timothy G. Clark","doi":"10.1016/j.molbrainres.2005.09.016","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Glucocorticoids<span><span> affect a variety of tissues to enable the organism to adapt to the stress. Hippocampal neurons contain glucocorticoid receptors and respond to elevated glucocorticoid levels by down-regulating the </span>HPA axis. Chronically, however, stress is deleterious to hippocampal neurons. Chronically elevated levels of glucocorticoids result in a decrease in the number of </span></span>dendritic spines<span>, reduced axonal growth and synaptogenesis<span>, and decreased neurogenesis<span> in the hippocampus. Tolloid-like 1 (</span></span></span></span><em>Tll-1</em><span>) is a metalloprotease<span> that potentiates the activity of the bone morphogenetic proteins (BMPs). Neurogenesis in the hippocampus of both developing and adult mammals requires BMPs. In this study, we demonstrate that </span></span><em>Tll-1</em> expression is increased in mice that have increased neurogenesis. The <em>Tll-1</em> promoter contains glucocorticoid response elements which are capable of binding to purified glucocorticoid receptor. Glucocorticoids decrease <em>Tll-1</em><span> expression in vitro. Finally, prenatal stress leads to a decrease in </span><em>Tll-1</em> mRNA expression in the hippocampus of adult female mice that is not observed in adult male mice indicating that Tll-1 expression is differentially regulated in males and females. The results of this study indicate that <em>Tll-1</em> is responsive to glucocorticoids and this mechanism might influence neurogenesis in the hippocampus.</p></div>","PeriodicalId":100932,"journal":{"name":"Molecular Brain Research","volume":"142 2","pages":"Pages 81-90"},"PeriodicalIF":0.0000,"publicationDate":"2005-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.molbrainres.2005.09.016","citationCount":"17","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Brain Research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169328X0500361X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 17
Abstract
Glucocorticoids affect a variety of tissues to enable the organism to adapt to the stress. Hippocampal neurons contain glucocorticoid receptors and respond to elevated glucocorticoid levels by down-regulating the HPA axis. Chronically, however, stress is deleterious to hippocampal neurons. Chronically elevated levels of glucocorticoids result in a decrease in the number of dendritic spines, reduced axonal growth and synaptogenesis, and decreased neurogenesis in the hippocampus. Tolloid-like 1 (Tll-1) is a metalloprotease that potentiates the activity of the bone morphogenetic proteins (BMPs). Neurogenesis in the hippocampus of both developing and adult mammals requires BMPs. In this study, we demonstrate that Tll-1 expression is increased in mice that have increased neurogenesis. The Tll-1 promoter contains glucocorticoid response elements which are capable of binding to purified glucocorticoid receptor. Glucocorticoids decrease Tll-1 expression in vitro. Finally, prenatal stress leads to a decrease in Tll-1 mRNA expression in the hippocampus of adult female mice that is not observed in adult male mice indicating that Tll-1 expression is differentially regulated in males and females. The results of this study indicate that Tll-1 is responsive to glucocorticoids and this mechanism might influence neurogenesis in the hippocampus.